A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526442



Internal ID15453735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14200165..14242983hg38UCSC Ensembl
Innerchr2:14340289..14383107hg19UCSC Ensembl
Innerchr2:14257740..14300558hg18UCSC Ensembl
Innerchr2:14290887..14333705hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3842819
hg1942819
hg1842819
hg1742819
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702745
Samples
Known GenesLINC00276
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526442
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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